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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720586Generated: November 1, 2026

Hydroxyamine hydrochloride → N-hydroxy-2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionamide

https://huagongshe.com/reaction/1720586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionateHCID 22907154—
SolventMethanolHCID 887—
ProductN-hydroxy-2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionamideHCID 15296597—

Reaction Steps

Methyl 2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionate (2.1 g, 6.01 mmol) is dissolved in methanol (20.0 mL). To this solution is added hydroxylamine hydrochloride (0.84 g, 12.0 mmol), followed by the addition of sodium methoxide (7.0 mL of a 4.37M solution). The reaction is stirred overnight at room temperature. The reaction is worked up by first removing all the solvent, and partitioning between ethyl acetate/hexane (2/1) and saturated sodium bicarbonate. The aqueous phase is extracted well with ethyl acetate/hexane, the combined organic layers are dried (MgSO4), and the solvent is evaporated. The product is purified by silica gel chromatography (ethyl acetate) to give N-hydroxy-2-[[4-methoxybenzenesulfonyl](benzyl)amino]propionamide, m.p. 149°-151° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506242
Source datasetuspto-grants-1996_04
ORD IDord-ea6d6735f56840c2b731d83307cf3d8c
Source noteuspto-grants-1996_04